Recalls distributed in Hawaii
These notices name Hawaii in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
1,551 stored notices name Hawaii, reported between Jun 27, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Hawaii too — those are in the archive.
Reported Jul 15, 2026
Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Jul 8, 2026
OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Access Systems, Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2026
Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
FDA (openFDA device enforcement)
Reported Jul 8, 2026
Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2026Updated Sep 16, 2026
Oribe Serene Scalp Densifying Shampoo, packaged in 8.5 fl. oz. (250 mL) bottles with UPC 840035231242 and 33.8 fl. oz.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.KAO USA Inc.
FDA (weekly enforcement report)
Reported Jul 8, 2026
Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog Number: ENF060182LD / 101033086…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medela Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2026
Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
FDA (openFDA device enforcement)
Reported Jul 8, 2026
GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2026Updated Sep 16, 2026
Determine HIV 1/2 Ag/Ab Combo 25T, Model/Catalog No. 7D2648
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Diagnostics Scarborough, Inc.
FDA (weekly enforcement report)
Reported Jul 1, 2026Updated Sep 16, 2026
Apheresis Red Blood Cells, Leukocytes Reduced
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blood Bank Of Hawaii
2 more products in this recall
FDA (weekly enforcement report)
Reported Jul 1, 2026
Dried Herring Fish 7 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Prime Food Processing LLC.
FDA (openFDA food enforcement)
Reported Jul 1, 2026
INZONE DETACHMENT SYSTEM, REF: M00345100950
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Jun 24, 2026
PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU
High riskUsing this product could cause serious injury, illness or death — stop using it now.Arrow International, LLC
34 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2026
azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISHABLE/KEEP FROZEN PRODUCT OF JAPAN DISTRIBUTED BY: AZUMA…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Azuma Foods International Inc. USA
FDA (openFDA food enforcement)
Reported Jun 24, 2026
iLet Bionic Pancreas, REF: BB1001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beta Bionics, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Mito Red Light, Super Mobile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mito Red Light Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product Description: The STAAR ICL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Staar Surgical AG
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Medical
FDA (openFDA device enforcement)
Reported Jun 17, 2026
NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan¿ SuperElastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.In2bones USA, LLC
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830
Moderate riskThis product could cause temporary or reversible health problems — stop using it.INSPIREMD Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
FDA (openFDA device enforcement)
Reported May 27, 2026
Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2026
Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.